Objective: To report fertility and pregnancy outcomes following transvaginal cervicoisthmic cerclage with a polypropylene sling during a previous pregnancy.

Methods: A continuous series of 57 women who underwent prophylactic cervicoisthmic cerclage during a previous (reference) pregnancy were enrolled. Telephone interviews were carried out to evaluate each patient's subsequent fertility.

Results: Among the 57 women interviewed, 8 had an inadequate follow-up, 13 women were lost to follow-up, 1 woman required a hemostatic hysterectomy, and 2 women required removal of the sling. Nineteen women did not desire a subsequent pregnancy. Of the 14 women who did desire a subsequent pregnancy, 1 woman had previously known tubal infertility. Of the 13 remaining women, 7 subsequently became pregnant. One woman had a spontaneous abortion (11 weeks of pregnancy); 1 woman delivered at 22 weeks of pregnancy, after a spontaneous premature membrane rupture; 1 woman had a cesarean delivery at 25 weeks of pregnancy; and 4 patients had a cesarean delivery after 37 weeks of pregnancy. Median duration of the 4 subsequent pregnancies at delivery was 37 weeks (interquartile range [IQR], 37-38 weeks). Median birth weight was 3040 g (IQR, 2500-3250 g).

Conclusion: Subsequent pregnancy is possible after transvaginal cervicoisthmic cerclage using a synthetic sling.

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http://dx.doi.org/10.1016/j.ijgo.2009.11.011DOI Listing

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Article Synopsis
  • * A total of 30 women participated, with successful results reported: a delivery rate of 93% and no pregnancy losses within 28 days post-procedure, though there was one surgical complication that was quickly addressed.
  • * The findings indicate that this modified technique is safe and effective for managing refractory cervical insufficiency, with promising results in preventing early pregnancy loss and maintaining fetal survival.
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This video-article describes a laparoscopic cervico-isthmic cerclage technique for managing cervical insufficiency in both pregnant and non-pregnant patients, utilizing a port-site closure device for precise suture placement. Two cases-one non-pregnant and one at 12 weeks gestation-underwent the procedure, with details on trocar placement, dissection, and suture passage documented. Both surgeries were completed successfully, with minimal blood loss and no complications.

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Updates on laparoscopic cervical cerclage: obstetric outcomes and surgical techniques.

Future Sci OA

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Department of Gynecology & Obstetrics, Hôtel-Dieu de France University Hospital, Saint Joseph University, Beirut, Lebanon.

Aim: Preterm birth is a worldwide health problem. After unsuccessful transvaginal cerclage, the transabdominal isthmo-cervical cerclage can be indicated. A laparoscopic approach has been described.

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To compare the maternal and fetal outcomes of women with cervical insufficiency (CI) undergoing McDonald cerclage (MC) and laparoscopic cervicoisthmic cerclage (LCC), so as to provide evidence for the selection of cerclage methods. A retrospective trial was carried out in the First Affiliated Hospital of Sun Yat-sen University from January 2010 to December 2020. A total of 221 women who underwent the prophylactic cerclage were divided into MC group (=54), LCC with MC history group (=28) and LCC without MC history group (=129) by the mode of operation and whether the pregnant women who underwent LCC had MC history.

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Isthmic retroperitoneal cerclage via vNOTES as a potential alternative to an abdominal cerclage: First technique description.

J Gynecol Obstet Hum Reprod

February 2023

The Department of Obstetrics and Gynecology, Imelda Hospital, Bonheiden, Belgium; KU Leuven-University of Leuven, Department of Development and Regeneration, Faculty of Medicine, Group Biomedical Sciences, UZ Herestraat 49 - box 902, 3000 Leuven, Belgium. Electronic address:

Objective: To describe a new technique for performing an isthmic retroperitoneal cerclage via vaginal Natural Orifice Transluminal Endoscopic Surgery (vNOTES).

Design: Stepwise explanation of the surgical technique using original video footage. This study was exempted from requiring hospital IRB.

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